List of variants in gene RPGR reported as uncertain significance for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_001034853.2(RPGR):c.865A>G (p.Ile289Val)	rs62640587	0.00005
NM_000328.3(RPGR):c.2066A>T (p.Asp689Val)	rs2147168869
NM_000328.3(RPGR):c.2149+4T>G	rs945212131
NM_001034853.2(RPGR):c.1286C>T (p.Pro429Leu)	rs2067408372
NM_001034853.2(RPGR):c.2180T>A (p.Met727Lys)
NM_001034853.2(RPGR):c.2254del (p.Glu752fs)	rs1060499897
NM_001034853.2(RPGR):c.2956_2957insA (p.Gly986fs)	rs1060499896
NM_001034853.2(RPGR):c.369C>G (p.Asp123Glu)	rs2147280505
NM_001034853.2(RPGR):c.878G>T (p.Arg293Met)

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